Pericak-Vance MA - Search Results

1

Analysis of linkage disequilibrium in gamma-aminobutyric acid receptor subunit genes in autistic disorder.

Martin ER, Menold MM, Wolpert CM, Bass MP, Donnelly SL, Ravan SA, Zimmerman A, Gilbert JR, Vance JM, Maddox LO, Wright HH, Abramson RK, DeLong GR, Cuccaro ML, Pericak-Vance MA. Martin ER, et al. Am J Med Genet. 2000 Feb 7;96(1):43-8. doi: 10.1002/(sici)1096-8628(20000207)96:1<43::aid-ajmg9>3.0.co;2-3. Am J Med Genet. 2000. PMID: 10686550

2

Genetic linkage studies in Huntington disease.

Pericak-Vance MA, Conneally PM, Merritt AD, Roos R, Norton JA Jr, Vance JM. Pericak-Vance MA, et al. Cytogenet Cell Genet. 1978;22(1-6):640-5. doi: 10.1159/000131042. Cytogenet Cell Genet. 1978. PMID: 156628 No abstract available.

3

Linkage of Tunisian autosomal recessive Duchenne-like muscular dystrophy to the pericentromeric region of chromosome 13q.

Ben Othmane K, Ben Hamida M, Pericak-Vance MA, Ben Hamida C, Blel S, Carter SC, Bowcock AM, Petruhkin K, Gilliam TC, Roses AD, et al. Ben Othmane K, et al. Nat Genet. 1992 Dec;2(4):315-7. doi: 10.1038/ng1292-315. Nat Genet. 1992. PMID: 1303286

4

Recombination of 4p16 DNA markers in an unusual family with Huntington disease.

Pritchard C, Zhu N, Zuo J, Bull L, Pericak-Vance MA, Vance JM, Roses AD, Milatovich A, Francke U, Cox DR, et al. Pritchard C, et al. Am J Hum Genet. 1992 Jun;50(6):1218-30. Am J Hum Genet. 1992. PMID: 1350884 Free PMC article.

5

Linkage studies in Charcot-Marie-Tooth disease type 2: evidence that CMT types 1 and 2 are distinct genetic entities.

Loprest LJ, Pericak-Vance MA, Stajich J, Gaskell PC, Lucas AM, Lennon F, Yamaoka LH, Roses AD, Vance JM. Loprest LJ, et al. Neurology. 1992 Mar;42(3 Pt 1):597-601. doi: 10.1212/wnl.42.3.597. Neurology. 1992. PMID: 1549221

6

North Carolina macular dystrophy is assigned to chromosome 6.

Small KW, Weber JL, Roses A, Lennon F, Vance JM, Pericak-Vance MA. Small KW, et al. Genomics. 1992 Jul;13(3):681-5. doi: 10.1016/0888-7543(92)90141-e. Genomics. 1992. PMID: 1639395

7

Localization of Charcot-Marie-Tooth disease type 1a (CMT1A) to chromosome 17p11.2.

Vance JM, Barker D, Yamaoka LH, Stajich JM, Loprest L, Hung WY, Fischbeck K, Roses AD, Pericak-Vance MA. Vance JM, et al. Genomics. 1991 Apr;9(4):623-8. doi: 10.1016/0888-7543(91)90355-i. Genomics. 1991. PMID: 1674726

8

Linkage studies in familial Alzheimer disease: evidence for chromosome 19 linkage.

Pericak-Vance MA, Bebout JL, Gaskell PC Jr, Yamaoka LH, Hung WY, Alberts MJ, Walker AP, Bartlett RJ, Haynes CA, Welsh KA, et al. Pericak-Vance MA, et al. Am J Hum Genet. 1991 Jun;48(6):1034-50. Am J Hum Genet. 1991. PMID: 2035524 Free PMC article.

9

Linkage studies of late-onset familial Alzheimer's disease.

Roses AD, Pericak-Vance MA, Clark CM, Gilbert JR, Yamaoka LH, Haynes CS, Speer MC, Gaskell PC, Hung WY, Trofatter JA, et al. Roses AD, et al. Adv Neurol. 1990;51:185-96. Adv Neurol. 1990. PMID: 2294655 No abstract available.

10

Confirmation of linkage in von Hippel-Lindau disease.

Vance JM, Small KW, Jones MA, Stajich JM, Yamaoka LH, Roses AD, Hung WY, Pericak-Vance MA. Vance JM, et al. Genomics. 1990 Mar;6(3):565-7. doi: 10.1016/0888-7543(90)90488-g. Genomics. 1990. PMID: 2328994

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